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Minnesota Retractor

EUDAMED

Class I (EU MDR)

Ref 1008-6

by Dental Expert

Identity

Trade Name
MINNESOTA RETRACTOR EUDAMED
Device Name
MINNESOTA RETRACTOR EUDAMED
Model / Reference
1008-6 EUDAMED

Identifiers

Primary DI / UDI-DI
D123100860 EUDAMED
Basic UDI-DI
++D12310086BU EUDAMED
EMDN Code
L150201 DENTAL RETRACTORS, REUSABLE EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Italy EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Implantable

No

EUDAMED

Reusable

Yes

EUDAMED

Contains Latex

No

EUDAMED

Reprocessed

No

EUDAMED

CMR Substance

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Endocrine Disruptor

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Minnesota Retractor by Dental Expert — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

Manufacturer
Dental Expert
EUDAMED SRN
PK-MF-000024595
Authorised Representative
ANTEX MEDI SOLUTION DE-AR-000008078

Sources (1)

  • EUDAMED 89df44e9-57f3-47e7-8782-b74ad4510bb4 61 fields · synced Jul 9, 2026